SMARTBLOCK PAIN PUMP
K-Number: K072053 · 2007-11-06
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Device Summary
Frequently Asked Questions
What is the SMARTBLOCK PAIN PUMP?
SMARTBLOCK PAIN PUMP is a medical device that received FDA 510(k) clearance on 2007-11-06. The listed applicant is Medical Flow Systems, Ltd.. The 510(k) number is K072053.
When did SMARTBLOCK PAIN PUMP receive FDA 510(k) clearance?
SMARTBLOCK PAIN PUMP received FDA 510(k) clearance on 2007-11-06, under 510(k) number K072053.
Who is the listed applicant for SMARTBLOCK PAIN PUMP?
The FDA 510(k) record lists Medical Flow Systems, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SMARTBLOCK PAIN PUMP?
The FDA product code for SMARTBLOCK PAIN PUMP is MEB.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MEB)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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